EP1264634A1 - Verwendung von Alkyl(ether)phosphaten(II) - Google Patents
Verwendung von Alkyl(ether)phosphaten(II) Download PDFInfo
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- EP1264634A1 EP1264634A1 EP01114066A EP01114066A EP1264634A1 EP 1264634 A1 EP1264634 A1 EP 1264634A1 EP 01114066 A EP01114066 A EP 01114066A EP 01114066 A EP01114066 A EP 01114066A EP 1264634 A1 EP1264634 A1 EP 1264634A1
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- Prior art keywords
- alkyl
- acid
- ether
- fatty
- phosphates
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/55—Phosphorus compounds
- A61K8/556—Derivatives containing from 2 to 10 oxyalkylene groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
Definitions
- the invention is in the field of emulsions and relates to the use of special phosphoric acid esters for the single-stage production of multiple emulsions, for example for cosmetics, textile technology or agriculture, a process for their Production and selected multiple emulsions.
- multiple emulsion is understood by the person skilled in the art to mean W / O emulsions which are in turn enclosed by a water phase or O / W emulsions which are in an oil matrix.
- Multiple emulsions are used today in the field of cosmetics when it comes to special sensory effects on the skin, as well as in agricultural engineering, for example in the production of effective pesticide concentrates.
- the preparation of these preparations is not easy, especially since two working steps have hitherto been necessary, ie in a first step the O / W or W / O emulsion has to be produced, which is then converted into the multiple emulsion in a second process.
- the object of the invention was therefore to provide multiple emulsions places that can be manufactured in one step and also with longer storage and high temperatures are stable. Finally, a wide variety of active ingredients should also be stable have it incorporated.
- the invention relates to the use of alkyl (ether) phosphates for the one-stage Production of multiple emulsions.
- Alkyl phosphates and alkyl ether phosphates - the term phosphoric acid ester is often used interchangeably - are known anionic emulsifiers, which are usually prepared by reacting longer-chain alcohols or their ethylene oxide addition products with phosphorus pentoxide or polyphosphorous acid, whereby the mono / diester ratio, which is important for the properties, via the Selection of the phosphating agent and the stoichiometric conditions of use is carried out.
- alkyl (ether) phosphates usually follow the formula (I) in which R 1 represents a linear or branched alkyl and / or alkenyl radical having 6 to 22 carbon atoms, R 2 and R 3 independently of one another represent hydrogen or likewise a linear or branched alkyl and / or alkenyl radical having 6 to 22 carbon atoms and Sum (m + n + p) means 0 or a number from 1 to 30.
- R 1 and R 2 are alkyl radicals having 12 to 18 carbon atoms, R 3 is hydrogen and the sum (m + n + p) is 0 of the numbers from 5 to 20.
- Typical examples are the Phosphatsammlungs inter of fatty alcohols, such as caproic alcohol, caprylic alcohol, capric alcohol, lauryl alcohol, myristyl alcohol, palmoleyl alcohol, cetyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, gadoleyl alcohol, Arachydylalkohol, behenyl alcohol and erucyl alcohol and the technical mixtures obtained by hydrogenation of corresponding fatty acid alkyl esters can be obtained.
- the use of alkyl phosphates or alkyl ether phosphates based on technical C 12 -C 18 or C 12 -C 14 coconut alcohol cuts is preferred.
- alkyl phosphates and alkyl ether phosphates can also be used, in particular those obtained by phosphating fatty alcohols and fatty alcohol polyglycol ethers together. It has proven to be advantageous to use alkyl (ether) phosphates, which are predominantly mono / diester mixtures, and which therefore have little or no proportion of triesters. Depending on the specific field of application, it may therefore be preferred to use products which are predominantly monoesters or diesters.
- the emulsifiers can be present in amounts of 1 to 15, preferably 2 to 10 and in particular 3 to 5% by weight, based on the multiple emulsions.
- the adducts of ethylene oxide and / or of propylene oxide with fatty alcohols, fatty acids, alkylphenols or with castor oil are known, commercially available products. These are mixtures of homologs whose average degree of alkoxylation is the ratio of the amounts of ethylene oxide and / or propylene oxide and substrate, with which the addition reaction is carried out.
- C 12/18 fatty acid monoesters and diesters of adducts of ethylene oxide with glycerol are known from DE 2024051 PS as refatting agents for cosmetic preparations.
- Alkyl and / or alkenyl oligoglycosides their preparation and their use are out known in the art. They are manufactured in particular through implementation of glucose or oligosaccharides with primary alcohols with 8 to 18 carbon atoms.
- glycoside residue both monoglycosides in which a cyclic sugar residue is glycosidically bound to the fatty alcohol, as well as oligomeric Glycosides with a degree of oligomerization of up to preferably about 8 are suitable.
- the degree of oligomerization is a statistical mean, one for such technical products are based on the usual homolog distribution.
- Alkyloligoglucoside are particularly preferred as co-emulsifiers, especially if they are production-related in a mixture with fatty alcohols.
- Typical examples of suitable partial glycerides are hydroxystearic acid monoglyceride, Hydroxystearic acid diglyceride, isostearic acid monoglyceride, isostearic acid diglyceride, Oleic acid monoglyceride, oleic acid diglyceride, ricinoleic acid moglyceride, ricinoleic acid diglyceride, Linoleic acid monoglyceride, linoleic acid diglyceride, linolenic acid monoglyceride, linolenic acid diglyceride, Erucic acid monoglyceride, erucic acid diglyceride, tartaric acid monoglyceride, Tartaric acid diglyceride, citric acid monoglyceride, citric diglyceride, malic acid monoglyceride, Malic acid diglyceride and their technical mixtures, the subordinate may still contain small amounts of triglyceride from the manufacturing process. Likewise Addition products of
- polyglycerol esters are polyglyceryl-2 dipolyhydroxystearates (Dehymuls® PGPH), polyglycerol-3-diisostearate (Lameform® TGI), polyglyceryl-4 Isostearate (Isolan® GI 34), polyglyceryl-3 oleates, diisostearoyl polyglyceryl-3 Diisostearate (Isolan® PDI), polyglyceryl-3 methylglucose distearate (Tego Care® 450), Polyglyceryl-3 Beeswax (Cera Bellina®), Polyglyceryl-4 Caprate (Polyglycerol Caprate T2010 / 90), Polyglyceryl-3 Cetyl Ether (Chimexane® NL), Polyglyceryl-3 Distearate (Cremophor® GS 32) and Polyglyceryl Polyricinoleate (Admul® WOL 1403) Polyglyceryl Dimerate is
- polyol esters examples include the mono-, di- and optionally reacted with 1 to 30 mol ethylene oxide Triester of trimethylolpropane or pentaerythritol with lauric acid, coconut fatty acid, Tallow fatty acid, palmitic acid, stearic acid, oleic acid, behenic acid and the like.
- polyol polyhydroxystearates especially polyglycerol polyhydroxystearate
- alkyl and / or alkyl oligoglycosides for example in a weight ratio of 25:75 to 75:25, such as those under the brand Eumulgin® VL75 (Cognis Deutschland GmbH) are on the market.
- Typical anionic emulsifiers are aliphatic fatty acids with 12 to 22 carbon atoms, such as palmitic acid, stearic acid or behenic acid, and dicarboxylic acids with 12 to 22 carbon atoms, such as azelaic acid or Sebacic acid.
- Zwitterionic surfactants can also be used as emulsifiers.
- Zwitterionic surfactants are those surface-active compounds which carry at least one quaternary ammonium group and at least one carboxylate and one sulfonate group in the molecule.
- Particularly suitable zwitterionic surfactants are the so-called betaines such as the N-alkyl-N, N-dimethylammonium glycinate, for example coconut alkyldimethylammonium glycinate, N-acylaminopropyl-N, N-dimethylammonium glycinate, for example coconut acylaminopropyldimethylammonium glycinate, and 2-alkyl-3-carboxylm -hydroxyethylimidazolines each having 8 to 18 carbon atoms in the alkyl or acyl group and the cocoacylaminoethylhydroxyethylcarboxymethylglycinate.
- betaines such as the N-alkyl-N, N-dimethylammonium glycinate, for example coconut alkyldimethylammonium glycinate, N-acylaminopropyl-N, N-dimethylammonium glycinate, for example
- Suitable emulsifiers are ampholytic surfactants.
- Ampholytic surfactants are surface-active compounds which, in addition to a C 8/18 alkyl or acyl group, contain at least one free amino group and at least one -COOH or -SO 3 H group in the molecule and are capable of forming internal salts.
- ampholytic surfactants are N-alkylglycine, N-alkylpropionic acid, N-alkylaminobutyric acid, N-alkyliminodipropionic acid, N-hydroxyethyl-N-alkylamidopropylglycine, N-alkyltaurine, N-alkyl sarcosine, 2-alkylaminopropionic acid and alkylaminoacetic acid each with about 8 to 18 carbon atoms in the alkyl group.
- Particularly preferred ampholytic surfactants are N-coconut alkylaminopropionate, coconut acylaminoethylaminopropionate and C 12/18 acyl sarcosine.
- cationic surfactants are also suitable as emulsifiers, those of the esterquat type, preferably methylquaternized difatty acid triethanolamine ester salts, being particularly preferred.
- mixtures of alk (en) yl oligoglycosides and polyol polyhydroxystearates already mentioned have proven to be particularly effective co-emulsifier systems
- mixtures of fatty alcohols, Fatty alcohol polyglycol ethers, partial glycerides and fatty acid esters have been proven For example under the brands Emulgade®® SE-PF and Emulgade CM (Cognis) im Are trade.
- the co-emulsifiers can be used in amounts of 5 to 15, preferably 7 to 10 wt .-% - based on the multiple emulsions - be included.
- Oil bodies are absolutely necessary for the production of emulsions, of course also multiple emulsions.
- esters of linear C 6 -C 22 fatty acids with branched alcohols in particular 2-ethylhexanol
- esters of C 18 -C 38 alkylhydroxycarboxylic acids with linear or branched C 6 -C 22 fatty alcohols cf.
- DE 19756377 A1 are suitable, in particular dioctyl malates, esters of linear and / or branched fatty acids with polyhydric alcohols (such as propylene glycol, dimer diol or trimer triol) and / or Guerbet alcohols, triglycerides based on C 6 -C 10 fatty acids, liquid mono- / di / triglyceride mixtures based on C 6 -C 18 fatty acids, esters of C 6 -C 22 fatty alcohols and / or Guerbet alcohols with aromatic carboxylic acids, in particular benzoic acid, esters of C 2 -C 12 dicarboxylic acids with linear or branched alcohols with 1 to 22 carbon atoms or polyols 2 to 10 carbon atoms and 2 to 6 hydroxyl groups, vegetable oils, branched primary alcohols, substituted cyclohexanes, linear and branched C 6 -C 22 fatty alcohol carbonates, such as Dic apryly
- Finsolv® TN linear or branched, symmetrical or asymmetrical dialkyl ethers with 6 to 22 carbon atoms per alkyl group, such as dicaprylyl ether (Cetiol® OE), ring opening products of epoxidized fatty acid esters with polyols, silicone oils (cyclomethicones, silicon methicone types, etc.) and / or aliphatic or naphthenic hydrocarbons, such as for example Squalane, squalene or dialkylcyclohexanes.
- Particularly stable multiple emulsions are obtained using vegetable glycerides and / or Guerbet alcohols, the use of which is therefore preferred.
- the oil bodies can be present in amounts of 10 to 25, preferably 12 to 20% by weight, based on the multiple emulsions.
- the multiple emulsions prepared using the alkyl (ether) phosphates can in turn for the production of cosmetic and / or pharmaceutical preparations, such as Hair shampoos, hair lotions, bubble baths, shower baths, creams, gels, lotions, alcoholic and aqueous / alcoholic solutions, emulsions, wax / fat masses, Stick preparations, powders or ointments are used.
- cosmetic and / or pharmaceutical preparations such as Hair shampoos, hair lotions, bubble baths, shower baths, creams, gels, lotions, alcoholic and aqueous / alcoholic solutions, emulsions, wax / fat masses, Stick preparations, powders or ointments are used.
- Anionic, nonionic, cationic and / or amphoteric or zwitterionic surfactants can be present as surface-active substances, the proportion of which in the compositions is usually about 1 to 70, preferably 5 to 50 and in particular 10 to 30% by weight.
- anionic surfactants are soaps, alkyl benzene sulfonates, alkane sulfonates, olefin sulfonates, alkyl ether sulfonates, glycerol ether sulfonates, ⁇ -methyl ester sulfonates, sulfo fatty acids, alkyl sulfates, fatty alcohol ether sulfates, glycerol ether sulfates, fatty acid ether sulfates, hydroxymischog sulfate sulfate, hydroxymischogether sulfate sulfate, hydroxymischogether sulfate sulfate, hydroxymischogether sulfate sulfate, hydroxymischogether sulfate sulfate, hydroxymischogether sulfate sulfate, hydroxymischogether sul
- nonionic surfactants are fatty alcohol polyglycol ethers, alkylphenol polyglycol ethers, fatty acid polyglycol esters, fatty acid amide polyglycol ethers, fatty amine polyglycol ethers, alkoxylated triglycerides, mixed ethers or mixed formals, optionally partially oxidized alk (en) yl oligoglycosides or especially glucoramide-acid-based vegetable derivatives, , Polyol fatty acid esters, sugar esters, sorbitan esters, polysorbates and amine oxides.
- nonionic surfactants contain polyglycol ether chains, they can have a conventional, but preferably a narrow, homolog distribution.
- cationic surfactants are quaternary ammonium compounds, such as, for example, dimethyldistearylammonium chloride, and esterquats, in particular quaternized fatty acid trialkanolamine ester salts.
- amphoteric or zwitterionic surfactants are alkyl betaines, alkyl amido betaines, aminopropionates, aminoglycinates, imidazolinium betaines and sulfobetaines. The surfactants mentioned are exclusively known compounds.
- Typical examples of particularly suitable mild, ie particularly skin-compatible, surfactants are fatty alcohol polyglycol ether sulfates, monoglyceride sulfates, mono- and / or dialkyl sulfosuccinates, fatty acid taurides, fatty acid glutamates, ⁇ -olefin sulfonates, ethercarboxylic acids, alkyl oligoglucosides, fatty acid glucamides, alkylamidobetaines, amphoacetals and / or protein fatty acid condensates, the latter preferably Wheat protein base.
- Typical examples of fats are glycerides, i.e. solid or liquid vegetable or animal Products consisting essentially of mixed glycerol esters of higher fatty acids
- waxes include natural waxes, e.g. Candelilla wax, carnauba wax, Japanese wax, Esparto grass wax, cork wax, guaruma wax, rice germ oil wax, sugar cane wax, Ouricury wax, montan wax, beeswax, shellac wax, walrus, lanolin (wool wax), Bürzelfett, Ceresin, Ozokerit (Erdwachs), Petrolatum, paraffin waxes, micro waxes; chemically modified waxes (hard waxes), e.g.
- Examples include natural lecithins Cephalins called, which are also called phosphatidic acids and derivatives of 1,2-diacyl-sn-glycerol-3-phosphoric acids represent.
- Phospholipids are usually mono- and preferably diesters of phosphoric acid with glycerin (Glycerol phosphates), which are generally classified as fats. Besides that come too Sphingosine or sphingolipids in question.
- Pearlescent waxes that can be used are, for example: alkylene glycol esters, especially ethylene glycol distearate; Fatty acid alkanolamides, especially coconut fatty acid diethanolamide; partial glycerides, especially stearic acid monoglyceride; Esters of polyvalent, optionally hydroxy-substituted Carboxylic acids with fatty alcohols with 6 to 22 carbon atoms, especially long-chain ones Esters of tartaric acid; Fatty substances, such as fatty alcohols, fatty ketones, fatty aldehydes, Fatty ethers and fatty carbonates, which have a total of at least 24 carbon atoms, especially lauron and distearyl ether; Fatty acids such as stearic acid, hydroxystearic acid or behenic acid, ring opening products of olefin epoxides having 12 to 22 carbon atoms with fatty alcohols with 12 to 22 carbon atoms and / or polyols with 2 to 15 Carbon atom
- the main consistency agents are fatty alcohols or hydroxy fatty alcohols from 12 to 22 and preferably 16 to 18 carbon atoms and in addition partial glycerides, fatty acids or hydroxy fatty acids.
- a combination of these substances with alkyl oligoglucosides is preferred and / or fatty acid N-methylglucamides of the same chain length and / or polyglycerol poly-12-hydroxystearates.
- Suitable thickeners are, for example, Aerosil types (hydrophilic silicas), polysaccharides, especially xanthan gum, guar guar, Agar-agar, alginates and tyloses, carboxymethyl cellulose and hydroxyethyl and hydroxypropyl cellulose, also higher molecular weight polyethylene glycol monoesters and diesters of fatty acids, Polyacrylates, (e.g. Carbopole® and Pemulen types from Goodrich; Synthalene® from Sigma; Keltrol types from Kelco; Seppic Sepigel types; Salcare types from Allied Colloids), Polyacrylamides, polymers, polyvinyl alcohol and polyvinyl pyrrolidone.
- Aerosil types hydrophilic silicas
- polysaccharides especially xanthan gum, guar guar, Agar-agar, alginates and tyloses, carboxymethyl cellulose and hydroxyethyl and hydroxypropyl cellulose, also higher mo
- Bentone® Gel VS-5PC (Rheox) proven which is a mixture of cyclopentasiloxane, disteardimonium hectorite and Is propylene carbonate.
- Surfactants such as ethoxylated are also suitable Fatty acid glycerides, esters of fatty acids with polyols such as pentaerythritol or Trimethylolpropane, fatty alcohol ethoxylates with a narrow homolog distribution or alkyl oligoglucosides and electrolytes such as table salt and ammonium chloride.
- Metal salts of fatty acids such as e.g. Magnesium, aluminum and / or Zinc stearate or ricinoleate can be used.
- Suitable cationic polymers are, for example, cationic cellulose derivatives, such as, for example, a quaternized hydroxyethyl cellulose, which is available under the name Polymer JR 400® from Amerchol, cationic starch, copolymers of diallylammonium salts and acrylamides, quaternized vinylpyrrolidone / vinylimidazole polymers, such as, for example, Luviquat® (BASF) , Condensation products of polyglycols and amines, quaternized collagen polypeptides, such as, for example, lauryldimonium hydroxypropyl hydrolyzed collagen (Lamequat®L / Grünau), quaternized wheat polypeptides, polyethyleneimine, cationic silicone polymers, such as, for example, amodimethicones, copolymers of adipic acid and dimethylaminetetrohydaminophenyl (hydroxymethyl) hydroxynoxydiamine
- Anionic, zwitterionic, amphoteric and nonionic polymers include, for example, vinyl acetate / crotonic acid copolymers, vinylpyrrolidone / vinyl acrylate copolymers, vinyl acetate / butyl maleate / isobornyl acrylate copolymers, methyl vinyl ether / maleic anhydride copolymers and their esters, uncrosslinked acrylamide acrylamide and non-crosslinked acrylamide acrylamide and polyamides, polyamide acrylamide and non-crosslinked acrylamide and polyamides with non-crosslinked acrylamide and polyamides Copolymers, octylacrylamide / methyl methacrylate / tert-butylaminoethyl methacrylate / 2-hydroxypropyl methacrylate copolymers, polyvinyl pyrrolidone, vinyl pyrrolidone / vinyl acetate copolymers, vinyl pyrrolidone / di
- Suitable silicone compounds are, for example, dimethylpolysiloxanes, methylphenylpolysiloxanes, cyclic silicones and amino, fatty acid, alcohol, polyether, epoxy, fluorine, glycoside and / or alkyl-modified silicone compounds, which can be both liquid and resinous at room temperature.
- Simethicones which are mixtures of dimethicones with an average chain length of 200 to 300 dimethylsiloxane units and hydrogenated silicates, are also suitable.
- a detailed overview of suitable volatile silicones can also be found by Todd et al. in Cosm.Toil. 91 , 27 (1976).
- benzoylmethane such as 1- (4'-tert-butylphenyl) -3- (4'-methoxyphenyl) propane-1,3-dione, 4-tert-butyl
- typical UV-A filters -4'methoxydibenzoylmethane Parsol® 1789
- 1-phenyl-3- (4'-isopropylphenyl) propane-1,3-dione and enamine compounds as described in DE 19712033 A1 (BASF).
- the UV-A and UV-B filters can of course also be used in mixtures.
- Particularly favorable combinations consist of the derivatives of benzoylmethane, e.g.
- water-soluble filters such as 2-phenylbenzimidazole-5-sulfonic acid and its alkali, alkaline earth, ammonium, alkylammonium, alkanolammonium and glucammonium salts.
- insoluble light protection pigments namely finely dispersed metal oxides or salts
- suitable metal oxides are, in particular, zinc oxide and titanium dioxide and, in addition, oxides of iron, zirconium, silicon, manganese, aluminum and cerium and mixtures thereof.
- Silicates (talc), barium sulfate or zinc stearate can be used as salts.
- the oxides and salts are used in the form of the pigments for skin-care and skin-protecting emulsions and decorative cosmetics.
- the particles should have an average diameter of less than 100 nm, preferably between 5 and 50 nm and in particular between 15 and 30 nm.
- the pigments can also be surface-treated, ie hydrophilized or hydrophobicized.
- Typical examples are coated titanium dioxides such as titanium dioxide T 805 (Degussa) or Eusolex® T2000 (Merck). Silicones, and in particular trialkoxyoctylsilanes or simethicones, are particularly suitable as hydrophobic coating agents. So-called micro- or nanopigments are preferably used in sunscreens. Micronized zinc oxide is preferably used.
- Other suitable UV light protection filters are in the overview by P.Finkel in S ⁇ FW-Journal 122 , 543 (1996) and Parf.Kosm. 3 , 11 (1999) .
- secondary light stabilizers of the antioxidant type can also be used, which interrupt the photochemical reaction chain which is triggered when UV radiation penetrates the skin.
- Typical examples are amino acids (e.g. glycine, histidine, tyrosine, tryptophan) and their derivatives, imidazoles (e.g. urocanic acid) and their derivatives, peptides such as D, L-carnosine, D-carnosine, L-carnosine and their derivatives (e.g. anserine) , Carotenoids, carotenes (e.g.
- ⁇ -carotene, ⁇ -carotene, lycopene and their derivatives, chlorogenic acid and their derivatives, lipoic acid and their derivatives (e.g. dihydroliponic acid), aurothioglucose, propylthiouracil and other thiols (e.g.
- thioredoxin glutathione, cysteine, cystine, Cystamine and their glycosyl, N-acetyl, methyl, ethyl, propyl, amyl, butyl and lauryl, palmitoyl, oleyl, ⁇ -linoleyl, cholesteryl and glyceryl esters) and their salts, dilauryl thiodipropionate , Distearylthiodipropionate, thiodipropionic acid and their derivatives (esters, ethers, peptides, lipids, nucleotides, nucleosides and salts) as well as sulfoximine compounds (e.g.
- buthioninsulfoximines homocysteine sulfoximine, butioninsulfones, penta-, hexa-, heptathioninsulfoximine
- noticeable dosages e.g. pmol to ⁇ mol / kg
- metal chelators e.g. ⁇ -hydroxy fatty acids, palmitic acid, phytic acid, lactoferrin
- ⁇ -hydroxy acids e.g. citric acid, lactic acid, malic acid
- humic acid bile acid, bile extracts, bilirubin, Biliverdin, EDTA, EGTA and their derivatives, unsaturated fatty acids and their derivatives (e.g.
- ⁇ -linolenic acid linoleic acid, oleic acid
- folic acid and their derivatives ubiquinone and ubiquinol and their derivatives
- vitamin C and derivatives e.g. ascorbyl palmitate, Mg-ascorbyl phosphate, ascorbyl acetate
- Tocopherols and derivatives e.g.
- vitamin E acetate
- vitamin A and derivatives vitamin A palmitate
- biogenic active ingredients are tocopherol, tocopherol acetate, tocopherol palmitate, Ascorbic acid, (deoxy) ribonucleic acid and its fragmentation products, ⁇ -glucans, Retinol, bisabolol, allantoin, phytantriol, panthenol, AHA acids, amino acids, Ceramides, pseudoceramides, essential oils, plant extracts such as e.g. Prunus extract, Bambaranus extract and understand vitamin complexes.
- Cosmetic deodorants counteract body odors, mask them or eliminate them.
- Body odors arise from the action of skin bacteria apocrine sweat, whereby unpleasant smelling breakdown products are formed. Accordingly contain deodorants active ingredients that act as germ inhibitors, enzyme inhibitors, Odor absorbers or odor maskers act.
- Esterase inhibitors are suitable as enzyme inhibitors. This is about it is preferably trialkyl citrates such as trimethyl citrate, tripropyl citrate, triisopropyl citrate, Tributyl citrate and especially triethyl citrate (Hydagen® CAT). Inhibit the substances enzyme activity and thereby reduce odor.
- trialkyl citrates such as trimethyl citrate, tripropyl citrate, triisopropyl citrate, Tributyl citrate and especially triethyl citrate (Hydagen® CAT). Inhibit the substances enzyme activity and thereby reduce odor.
- esterase inhibitors are sterol sulfates or phosphates, such as for example lanosterol, cholesterol, campesterol, stigmasterol and sitosterol sulfate or phosphate, dicarboxylic acids and their esters, such as glutaric acid, Monoethyl glutarate, diethyl glutarate, adipic acid, monoethyl adipate, Diethyl adipate, malonic acid and diethyl malonate, hydroxycarboxylic acids and their esters such as citric acid, malic acid, tartaric acid or tartaric acid diethyl ester, and zinc glycinate.
- dicarboxylic acids and their esters such as glutaric acid, Monoethyl glutarate, diethyl glutarate, adipic acid, monoethyl adipate, Diethyl adipate, malonic acid and diethyl malonate
- Substances which absorb odor-forming compounds are suitable as odor absorbers and can hold on to a large extent. They reduce the partial pressure of the individual components and thus reduce their speed of propagation. It is important that Perfumes must remain unaffected. Odor absorbers have no effectiveness against bacteria. For example, they contain a complex zinc salt as the main component the ricinoleic acid or special, largely odorless fragrances that the Are known in the art as "fixators" such. B. extracts of Labdanum or Styrax or certain abietic acid derivatives. Fragrances or act as odor maskers Perfume oils that, in addition to their function as odor maskers, deodorants their give each fragrance note. Mixtures may be mentioned as perfume oils from natural and synthetic fragrances.
- Natural fragrances are extracts of flowers, stems and leaves, fruits, fruit peels, roots, woods, herbs and grasses, needles and twigs as well as resins and balms. Furthermore come animal Raw materials in question, such as civet and castoreum.
- Typical synthetic Fragrance compounds are products of the ester, ether, aldehyde, ketone, Alcohols and hydrocarbons. Fragrance compounds of the ester type are e.g.
- ethers include, for example, benzyl ethyl ether, the aldehydes e.g.
- the linear Alkanals with 8 to 18 carbon atoms citral, citronellal, citronellyloxyacetaldehyde, Cyclamenaldehyde, Hydroxycitronellal, Lilial and Bourgeonal, to the ketones e.g. the Jonone and methyl cedryl ketone, to the alcohols anethole, citronellol, eugenol, isoeugenol, Geraniol, linalool, phenylethyl alcohol and terpineol, to the hydrocarbons belong mainly to the terpenes and balms. However, mixtures are preferred different fragrances are used, which together produce an appealing fragrance.
- perfume oils e.g. Sage oil, chamomile oil, clove oil, lemon balm oil, Mint oil, cinnamon leaf oil, linden blossom oil, juniper berry oil, vetiver oil, oliban oil, Galbanum oil, Labdanum oil and Lavandin oil.
- water-soluble additives are e.g. Preservatives, water-soluble fragrances, pH value adjusting agents, e.g. Buffer mixtures, water soluble thickeners, e.g. water-soluble natural or synthetic polymers such as Xanthan gum, hydroxyethyl cellulose, polyvinyl pyrrolidone or high molecular weight polyethylene oxides.
- Common film formers are, for example, chitosan, microcrystalline chitosan, quaternized Chitosan, polyvinylpyrrolidone, vinylpyrrolidone-vinyl acetate copolymers, polymers the acrylic acid series, quaternary cellulose derivatives, collagen, hyaluronic acid or its salts and similar compounds.
- Piroctone olamine (1-hydroxy-4-methyl-6- (2,4,4-trimythylpentyl) -2- (1H) -pyridinone monoethanolamine salt) comes as antidandruff active substances, Baypival® (Climbazole), Ketoconazol®, (4-acetyl-1 - ⁇ - 4- [2- (2.4-dichlorophenyl) r-2- (1H-imidazol-1-ylmethyl) -1,3-dioxylan-c-4-ylmethoxyphenyl ⁇ piperazine, Ketoconazole, elubiol, selenium disulfide, sulfur colloidal, sulfur polyethylene glycol sorbitan monooleate, Sulfuric ricinole polyoxide, sulfur tar distillates, Salicylic acid (or in combination with hexachlorophene), undexylenic acid monoethanolamide Sulfosuccinate Na salt, Lamepon® UD (protein undecylenic acid con
- Montmorillonites, clay minerals, pemulene and alkyl-modified carbopol types can serve as swelling agents for aqueous phases. Further suitable polymers or swelling agents can be found in the overview by R. Lochhead in Cosm.Toil. 108 , 95 (1993) .
- N, N-diethyl-m-toluamide, 1,2-pentanediol or ethyl butylacetylaminopropionate come as insect repellents in question
- Dihydroxyacetone is suitable as a self-tanner.
- tyrosine inhibitors that prevent the formation of Preventing melanin and finding application in depigmenting agents come, for example Arbutin, ferulic acid, kojic acid, coumaric acid and ascorbic acid (vitamin C) are possible.
- Suitable preservatives are, for example, phenoxyethanol, formaldehyde solution, Parabens, pentanediol or sorbic acid as well as those known under the name Surfacine® Silver complexes and those listed in Appendix 6, Parts A and B of the Cosmetics Ordinance other substance classes.
- Perfume oils include mixtures of natural and synthetic fragrances. Natural fragrances are extracts of flowers (lily, lavender, rose, jasmine, neroli, y-lang-ylang), Stems and leaves (geranium, patchouli, petitgrain), fruits (anise, coriander, Caraway, juniper), fruit peel (bergamot, lemon, oranges), roots (mace, Angelica, Celery, Cardamom, Costus, Iris, Calmus), Woods (Pine, Sandal, Guaiac, Cedarwood, rosewood), herbs and grasses (tarragon, lemongrass, sage, thyme), needles and twigs (spruce, fir, pine, mountain pine), resins and balsams (Galbanum, Elemi, Benzoin, myrrh, olibanum, opoponax).
- Typical synthetic fragrance compounds are Products of the ester, ether, aldehyde, ketone, alcohol and hydrocarbon type. Fragrance compounds of the ester type are e.g.
- the ethers include, for example, benzyl ethyl ether the aldehydes e.g.
- the linear alkanals with 8 to 18 carbon atoms citral, citronellal, Citronellyloxyacetaldehyde, Cyclamenaldehyde, Hydroxycitronellal, Lilial and Bourgeonal, too the ketones e.g. the Jonone, ⁇ -isomethylionon and methylcedrylketone, to the alcohols Anethole, citronellol, eugenol, isoeugenol, geraniol, linalool, phenylethyl alcohol and terpineol,
- the hydrocarbons mainly include the terpenes and balms.
- Aroma components are used as perfume oils, e.g. Sage oil, chamomile oil, Clove oil, lemon balm oil, mint oil, cinnamon leaf oil, linden blossom oil, juniper berry oil, vetiver oil, Oliban oil, galbanum oil, labolanum oil and lavandin oil.
- the flavors include, for example, peppermint oil, spearmint oil, anise oil, star anise oil, caraway oil, Eucalyptus oil, fennel oil, lemon oil, wintergreen oil, clove oil, menthol and the like in question.
- the dyes which can be used are those substances which are suitable and approved for cosmetic purposes, as compiled, for example, in the publication "Cosmetic Dyes” by the Dye Commission of the German Research Foundation, Verlag Chemie, Weinheim, 1984, pp . 81-106 . Examples are culinary red A (CI 16255), patent blue V (CI42051), indigotine (CI73015), chlorophyllin (CI75810), quinoline yellow (CI47005), titanium dioxide (CI77891), indanthrene blue RS (CI 69800) and madder varnish (CI58000). Luminol may also be present as the luminescent dye. These dyes are usually used in concentrations of 0.001 to 0.1% by weight, based on the mixture as a whole.
- the total proportion of auxiliaries and additives can be 1 to 50, preferably 5 to 40% by weight. based on the mean - amount.
- the preparation of the agents can be done by conventional cold or Hot processes take place; the phase inversion temperature method is preferably used.
- Droplet size and emulsion stability composition 1 2 3 4 5 6 V1 V2 Eumulgin® VL 75 Polyglyceryl-2 dipolyhydroxystearate (and) Cocoglucosides 5.0 5.0 - - - - 8.0 - Emulgade® SE-PF Glyceryl Stearate (and) Ceteareth-20 (and) Ceteareth-12 (and) Ceterayl Alcohol (and) Cetyl Palmitate - - 7.5 7.5 - - - 10.0 Emulgade® CM Cetearyl Isononanoate (and) Ceteareth-20 (and) Cetearyl Alcohol (and) Cetearyl Stearate (and) Glycerol (and) Ceteareth-12 (and) Cetyl Palmitate - - - 7.5 7.5 - - Cutina® MD Glyceryl distearate 3.0 3.0 3.0 3.0 3.0 3.0 3.0 Myritol® 331 Coco Glycerides 12.
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- Animal Behavior & Ethology (AREA)
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Abstract
Description
- (a) Alkyl(ether)phosphate,
- (b1) Alkyl- und/oder Alkenyloligoglykoside und Polyolpolyhydroxysterate und/oder
- (b2) Fettalkohole, Fettalkoholpolyglycolether, Partialglyceride und Fettsäureester,
- (c) pflanzliche Glyceride und/oder Guerbetalkohole und
- (d) Wasser
- (a) 1 bis 10, vorzugsweise 2 bis 5 Gew.-% Alkyl(ether)phosphate,
- (b1) 1 bis 15, vorzugsweise 5 bis 10 Gew.-% Alkyl- und/oder Alkenyloligoglykoside und Polyolpolyhydroxysterate und/oder
- (b2) 1 bis 15, vorzugsweise 5 bis 10 Gew.-% Fettalkohole, Fettalkoholpolyglycolether, Partialglyceride und Fettsäureester,
- (c) 5 bis 25, vorzugsweise 10 bis 20 Gew.-% pflanzliche Glyceride und/oder Guerbetalkohole
Tröpfchengröße und Emulsionsstabilität | ||||||||
Zusammensetzung | 1 | 2 | 3 | 4 | 5 | 6 | V1 | V2 |
Eumulgin® VL 75 Polyglyceryl-2 Dipolyhydroxystearat (and) Cocoglucosides | 5,0 | 5,0 | - | - | - | - | 8,0 | - |
Emulgade® SE-PF Glyceryl Stearate (and) Ceteareth-20 (and) Ceteareth-12 (and) Ceterayl Alcohol (and) Cetyl Palmitate | - | - | 7,5 | 7,5 | - | - | - | 10,0 |
Emulgade® CM Cetearyl Isononanoate (and) Ceteareth-20 (and) Cetearyl Alcohol (and) Cetearyl Stearat (and) Glycerol (and) Ceteareth-12 (and) Cetyl Palmitate | - | - | - | - | 7,5 | 7,5 | - | - |
Cutina® MD Glyceryl Distearate | 3,0 | 3,0 | 3,0 | 3,0 | 3,0 | 3,0 | 3,0 | 3,0 |
Myritol® 331 Coco Glycerides | 12,0 | - | 12,0 | - | 12,0 | - | 12,0 | - |
Eutanol® G Octyldodecanol | - | 12,0 | - | 12,0 | - | 12,0 | - | 12,0 |
Crafol® AP56 Sodium Dodecyl Phosphate | 3,3 | 3,3 | 3,3 | 3,3 | 3,3 | 3,3 | 3,3 | 3,3 |
Glycerol | 3,0 | 3,0 | 3,0 | 3,0 | 3,0 | 3,0 | 3,0 | 3,0 |
Wasser | ad 100 | |||||||
Stabilität | ||||||||
- nach 1 w, 20 °C | + | + | + | + | + | + | + | + |
- nach 1 w, 40 °C | + | + | + | + | + | + | + | + |
- nach 4 w, 20 °C | + | + | + | + | + | + | - | - |
- nach 4 w, 40 °C | + | + | + | + | + | + | - | - |
Claims (10)
- Verwendung von Alkyl(ether)phosphaten als Emulgatoren zur einstufigen Herstellung von multiple Emulsionen.
- Verwendung nach Anspruch 1, dadurch gekennzeichnet, dass man Alkyl(ether)-phosphate der Formel (I) einsetzt, in der R1 für einen linearen oder verzweigten Alkyl- und/oder Alkenylrest mit 6 bis 22 Kohlenstoffatomen, R2 und R3 unabhängig voneinander für Wasserstoff oder ebenfalls einen linearen oder verzweigten Alkyl- und/oder Alkenylrest mit 6 bis 22 Kohlenstoffatomen steht sowie die Summe (m+n+p) 0 oder eine Zahl von 1 bis 30 bedeutet.
- Verwendung nach den Ansprüchen 1 und/oder 2, dadurch gekennzeichnet, dass man Alkyl(ether)phosphate einsetzt, bei denen es sich überwiegend um Mono/Diester-Gemische handelt.
- Verwendung nach mindestens einem der Ansprüche 1 bis 3, dadurch gekennzeichnet, dass man Alkyl(ether)phosphate einsetzt, bei denen es sich überwiegend um Monoester handelt.
- Verwendung nach mindestens einem der Ansprüche 1 bis 4, dadurch gekennzeichnet, dass man Alkyl(ether)phosphate einsetzt, bei denen es sich überwiegend um Diester handelt.
- Verwendung nach mindestens einem der Ansprüche 1 bis 5, dadurch gekennzeichnet, dass man als Co-Emulgatoren Mischungen von Alkyl- und/oder Alkenyloligoglykosiden mit Polyolpolyhydroxystearaten einsetzt.
- Verwendung nach mindestens einem der Ansprüche 1 bis 5, dadurch gekennzeichnet, dass man als Co-Emulgatoren Mischungen von Fettalkoholen, Fettalkoholpolyglycolethern, Partialglyceriden und Fettsäureestern einsetzt.
- Verwendung nach mindestens einem der Ansprüche 1 bis 7, dadurch gekennzeichnet, dass man als Ölkörper Glyceridgemische und/oder Guerbetalkohole einsetzt.
- Verfahren zur einstufigen Herstellung von multiplen Emulsionen, dadurch gekennzeichnet, dass man(a) Alkyl(ether)phosphate,(b1) Alkyl- und/oder Alkenyloligoglykoside und Polyolpolyhydroxysterate und/oder(b2) Fettalkohole, Fettalkoholpolyglycolether, Partialglyceride und Fettsäureester,(c) pflanzliche Glyceride und/oder Guerbetalkohole und(d) Wasser
- Multiple Emulsionen, enthaltend(a) Alkyl(ether)phosphate,(b1) Alkyl- und/oder Alkenyloligoglykoside und Polyolpolyhydroxysterate und/oder(b2) Fettalkohole, Fettalkoholpolyglycolether, Partialglyceride und Fettsäureester,(c) pflanzliche Glyceride und/oder Guerbetalkohole und(d) Wasser.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE50105061T DE50105061D1 (de) | 2001-06-08 | 2001-06-08 | Verwendung von Alkyl(ether)phosphaten |
EP01114066A EP1264634B1 (de) | 2001-06-08 | 2001-06-08 | Verwendung von Alkyl(ether)phosphaten |
AT01114066T ATE286779T1 (de) | 2001-06-08 | 2001-06-08 | Verwendung von alkyl(ether)phosphaten |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP01114066A EP1264634B1 (de) | 2001-06-08 | 2001-06-08 | Verwendung von Alkyl(ether)phosphaten |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1264634A1 true EP1264634A1 (de) | 2002-12-11 |
EP1264634B1 EP1264634B1 (de) | 2005-01-12 |
Family
ID=8177684
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP01114066A Expired - Lifetime EP1264634B1 (de) | 2001-06-08 | 2001-06-08 | Verwendung von Alkyl(ether)phosphaten |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP1264634B1 (de) |
AT (1) | ATE286779T1 (de) |
DE (1) | DE50105061D1 (de) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1449516A1 (de) * | 2003-02-21 | 2004-08-25 | Beiersdorf AG | Kosmetische und dermatologische Emulsionen Phosphorsäureester enthaltend |
EP1608327A2 (de) * | 2003-03-14 | 2005-12-28 | Smithkline Beecham Corporation | Zusammensetzungen und verfahren zur verhinderung von zahnverfärbung |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5391321A (en) * | 1992-03-04 | 1995-02-21 | Th. Goldschmidt Ag | Liquid or pasty, storage-stable multiple emulsions of the O1 /W/O.sup.2 |
DE19631792A1 (de) * | 1996-08-08 | 1997-03-20 | Henkel Kgaa | Sonnenschutzmittel |
EP0780112A1 (de) * | 1995-12-21 | 1997-06-25 | Beiersdorf Aktiengesellschaft | Verfahren zur Herstellung von O/W- oder O/W/O-Emulsionen sowie nach solchen Verfahren erhältliche O/W- und O/W/O-Emulsionen |
DE19632043A1 (de) * | 1996-08-08 | 1998-02-12 | Henkel Kgaa | Sonnenschutzmittel |
EP1013338A1 (de) * | 1998-12-23 | 2000-06-28 | L'oreal | Nanoemulsion aus Fettsäureestern von Phosphorsäure und deren Verwendung in Kosmetika, Dermatologie, Pharmazeutika und/oder Ophthalmologie |
-
2001
- 2001-06-08 EP EP01114066A patent/EP1264634B1/de not_active Expired - Lifetime
- 2001-06-08 AT AT01114066T patent/ATE286779T1/de not_active IP Right Cessation
- 2001-06-08 DE DE50105061T patent/DE50105061D1/de not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5391321A (en) * | 1992-03-04 | 1995-02-21 | Th. Goldschmidt Ag | Liquid or pasty, storage-stable multiple emulsions of the O1 /W/O.sup.2 |
EP0780112A1 (de) * | 1995-12-21 | 1997-06-25 | Beiersdorf Aktiengesellschaft | Verfahren zur Herstellung von O/W- oder O/W/O-Emulsionen sowie nach solchen Verfahren erhältliche O/W- und O/W/O-Emulsionen |
DE19631792A1 (de) * | 1996-08-08 | 1997-03-20 | Henkel Kgaa | Sonnenschutzmittel |
DE19632043A1 (de) * | 1996-08-08 | 1998-02-12 | Henkel Kgaa | Sonnenschutzmittel |
EP1013338A1 (de) * | 1998-12-23 | 2000-06-28 | L'oreal | Nanoemulsion aus Fettsäureestern von Phosphorsäure und deren Verwendung in Kosmetika, Dermatologie, Pharmazeutika und/oder Ophthalmologie |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1449516A1 (de) * | 2003-02-21 | 2004-08-25 | Beiersdorf AG | Kosmetische und dermatologische Emulsionen Phosphorsäureester enthaltend |
EP1608327A2 (de) * | 2003-03-14 | 2005-12-28 | Smithkline Beecham Corporation | Zusammensetzungen und verfahren zur verhinderung von zahnverfärbung |
Also Published As
Publication number | Publication date |
---|---|
ATE286779T1 (de) | 2005-01-15 |
DE50105061D1 (de) | 2005-02-17 |
EP1264634B1 (de) | 2005-01-12 |
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